PROMPT: Providing Mental Health Precision Treatment

Sponsor
University of Michigan (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT04342494
Collaborator
(none)
4,500
1
5
34.6
130.1

Study Details

Study Description

Brief Summary

This research study is being conducted to understand if patients benefit from mobile health interventions while waiting for in-clinic mental health treatments, and to understand which patients receive the most benefit.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Enhanced Feedback + Standard Feedback
  • Device: Headspace app + Standard Feedback
  • Device: Headspace app + Enhanced Feedback + Standard Feedback
  • Device: SilverCloud + Standard Feedback
  • Device: SilverCloud app +Enhanced Feedback +Standard Feedback
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
4500 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
Providing Mental Health Precision Treatment
Actual Study Start Date :
May 13, 2020
Anticipated Primary Completion Date :
Apr 1, 2023
Anticipated Study Completion Date :
Apr 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Enhanced Feedback + Standard Feedback

Participants will receive enhanced feedback from the MyDataHelps study app in addition to standard feedback from the activity tracker.

Behavioral: Enhanced Feedback + Standard Feedback
Standard Feedback (SF) All participants will receive the standard feedback that is standard feedback from the activity trackers. Feedback includes activity level, heart rate, and progress toward daily activity goals on the device itself. Enhanced Feedback (EF) Participants randomized to receive enhanced feedback will receive this feedback from the MyDataHelps study app. This includes varying types of text and visual feedback based on data collected through the app. Feedback will be displayed to participants on a dashboard in the app or delivered via pop-up notifications. Participants will receive a combination of text and visual feedback.

Experimental: Headspace app + Standard Feedback

Participants will receive an app-based intervention in addition to standard feedback from the activity tracker.

Device: Headspace app + Standard Feedback
Standard Feedback (SF) All participants will receive the standard feedback that is standard feedback from the activity trackers. Feedback includes activity level, heart rate, and progress toward daily activity goals on the device itself. Headspace is an app designed to train the user in mindfulness practices.

Experimental: Headspace app + Enhanced Feedback + Standard Feedback

Participants will receive an app-based intervention, enhanced feedback from the MyDataHelps study app, and standard feedback activity tracker.

Device: Headspace app + Enhanced Feedback + Standard Feedback
Standard Feedback (SF) All participants will receive the standard feedback that is standard feedback from the activity trackers. Feedback includes activity level, heart rate, and progress toward daily activity goals on the device itself. Enhanced Feedback (EF) Participants randomized to receive enhanced feedback will receive this feedback from the MyDataHelps study app. This includes varying types of text and visual feedback based on data collected through the app. Feedback will be displayed to participants on a dashboard in the app or delivered via pop-up notifications. Participants will receive a combination of text and visual feedback. Headspace is an app designed to train the user in mindfulness practices.

Experimental: SilverCloud app + Standard Feedback

Participants will receive an app-based intervention in addition to standard feedback from the activity tracker.

Device: SilverCloud + Standard Feedback
Standard Feedback (SF) All participants will receive the standard feedback that is standard feedback from the activity trackers. Feedback includes activity level, heart rate, and progress toward daily activity goals on the device itself. Silvercloud is an app designed to deliver cognitive behavioral therapy.

Experimental: SilverCloud app +Enhanced Feedback +Standard Feedback

Participants will receive an app-based intervention, enhanced feedback from the MyDataHelps study app, and standard feedback from the activity tracker.

Device: SilverCloud app +Enhanced Feedback +Standard Feedback
Standard Feedback (SF) All participants will receive the standard feedback that is standard feedback from the activity trackers. Feedback includes activity level, heart rate, and progress toward daily activity goals on the device itself. Enhanced Feedback (EF) Participants randomized to receive enhanced feedback will receive this feedback from the MyDataHelps study app. This includes varying types of text and visual feedback based on data collected through the app. Feedback will be displayed to participants on a dashboard in the app or delivered via pop-up notifications. Participants will receive a combination of text and visual feedback. Silvercloud is an app designed to deliver cognitive behavioral therapy.

Outcome Measures

Primary Outcome Measures

  1. Depression as measured by the Patient Health Questionnaire 9(PHQ-9) [Up to 12 months]

    The PHQ-9 is a multipurpose instrument for screening, diagnosing, monitoring and measuring the severity of depression: The PHQ-9 incorporates self-report questions on 9 specific depression symptoms that align with the DSM-IV depression diagnostic criteria. PHQ-9 scores range from 0-27 and 27 indicates severe depression.

Secondary Outcome Measures

  1. Mood as measured by the Mental Health App Assessment [Daily up to about 12 months]

    Single Question, "On a scale of 1 to 10, what was your average mood today?" Scores will be averaged over follow-up periods with lower scores indicating worse moods and higher scores indicating better moods.

  2. Suicide risk as measured by the Positive and Negative Suicide Ideation Inventory (PANSI) [Up to 12 months]

    This is a 14-item subjectively completed inventory that consisted of 2 subscales: the PANSI-NSI subscale composed of 8 items and the Positive Ideation (PANSI-PI) subscale consisting of 6 items. The possible total scores on the PANSI-NSI and PANSI-PI subscales range from 8 to 40 and 6 to 30, respectively. Higher scores on the PANSI-NSI and lower scores on the PANSI-PI reflect greater risk for suicidal behavior.

  3. Anxiety as measured using the Generalized Anxiety Disorder 7-Item (GAD-7) Scale [Up to 12 months]

    GAD-7 consists total score for the seven items ranges from 0 to 21. Scores of 5, 10, and 15 represent cut points for mild, moderate, and severe anxiety, respectively.

  4. Substance use as measured by the Alcohol, Smoking, and Substance Involvement Screening Test (ASSIST) [Up to 12 months]

    The ASSIST Global Continuum of Illicit Drug Risk Score ranges from 0 to 308, with higher scores indicating greater risk.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Must have a scheduled mental health intake appointment at Michigan Medicine Outpatient Psychiatry or University Health Service at the University of Michigan

  • Must have daily access to a smartphone version that is compatible with study activity trackers.

  • Understands English to enable consent and use of the MyDataHelps app and app-based interventions

  • Provide complete, updated contact information upon enrollment to the study

  • Agree to be contacted by study staff during the study

  • Willingness to keep study setup (devices, apps, settings) in required configuration for the duration of the study, and following instructions by study staff if required to update or re-achieve required configuration if required configuration has been lost (e.g., change of phone, app deletion)

Exclusion Criteria:
  • Self-reported or medical record indication of a current eating disorder

  • Scheduled outpatient mental health appointment is a pediatric appointment (even if age 18+)

  • Wrist too large or too small to wear an Apple Watch or Fitbit comfortably (Note: bands that are shorter or longer than the standard will be made available to minimize this exclusion)

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Michigan Ann Arbor Michigan United States 48109

Sponsors and Collaborators

  • University of Michigan

Investigators

  • Principal Investigator: Amy Bohnert, University of Michigan

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Amy S.B. Bohnert, Associate Professor, University of Michigan
ClinicalTrials.gov Identifier:
NCT04342494
Other Study ID Numbers:
  • HUM00164162
First Posted:
Apr 13, 2020
Last Update Posted:
Dec 8, 2021
Last Verified:
Dec 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
Yes
Product Manufactured in and Exported from the U.S.:
Yes
Keywords provided by Amy S.B. Bohnert, Associate Professor, University of Michigan
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 8, 2021